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Computationally Reconstructing Cotranscriptional RNA Folding Pathways from Experimental Data Reveals Rearrangement of Non-Native Folding Intermediates

View ORCID ProfileAngela M Yu, Paul M. Gasper, View ORCID ProfileEric J. Strobel, View ORCID ProfileKyle E. Watters, View ORCID ProfileAlan A. Chen, View ORCID ProfileJulius B. Lucks
doi: https://doi.org/10.1101/379222
Angela M Yu
1Tri-Institutional Program in Computational Biology and Medicine, Weill Cornell Medicine, New York, NY 10065
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Paul M. Gasper
2Department of Chemistry and the RNA Institute, University at Albany, 1400 Washington Ave, Albany, NY 12222
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Eric J. Strobel
3Department of Chemical and Biological Engineering, Northwestern University, 2145 Sheridan Rd., Evanston, Il 60201
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Kyle E. Watters
4Department of Molecular and Cell Biology, University of California Berkeley, 731 Stanley Hall, Berkeley, CA 94720
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Alan A. Chen
2Department of Chemistry and the RNA Institute, University at Albany, 1400 Washington Ave, Albany, NY 12222
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Julius B. Lucks
3Department of Chemical and Biological Engineering, Northwestern University, 2145 Sheridan Rd., Evanston, Il 60201
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Summary

The series of RNA folding events that occur during transcription, or a cotranscriptional folding pathway, can critically influence the functional roles of RNA in the cell. Here we present a method, Reconstructing RNA Dynamics from Data (R2D2), to uncover details of cotranscriptional folding pathways by predicting RNA secondary and tertiary structures from cotranscriptional SHAPE-Seq data. We applied R2D2 to the folding of the Escherichia coli Signal Recognition Particle (SRP) RNA sequence and show that this sequence undergoes folding through non-native intermediate structures that require significant structural rearrangement before reaching the functional native structure. Secondary structure folding pathway predictions and all-atom molecular dynamics simulations of folding intermediates suggest that this rearrangement can proceed through a toehold mediated strand displacement mechanism, which can be disrupted and rescued with point mutations. These results demonstrate that even RNAs with simple functional folds can undergo complex folding processes during synthesis, and that small variations in their sequence can drastically affect their cotranscriptional folding pathways.

Highlights

  • - Computational methods predict RNA structures from cotranscriptional SHAPE-Seq data

  • - The E. coli SRP RNA folds into non-native structural intermediates cotranscriptionally

  • - These structures rearrange dynamically to form an extended functional fold

  • - Point mutations can disrupt and rescue cotranscriptional RNA folding pathways

Footnotes

  • Lead Contact – Julius B. Lucks

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted July 28, 2018.
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Computationally Reconstructing Cotranscriptional RNA Folding Pathways from Experimental Data Reveals Rearrangement of Non-Native Folding Intermediates
Angela M Yu, Paul M. Gasper, Eric J. Strobel, Kyle E. Watters, Alan A. Chen, Julius B. Lucks
bioRxiv 379222; doi: https://doi.org/10.1101/379222
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Computationally Reconstructing Cotranscriptional RNA Folding Pathways from Experimental Data Reveals Rearrangement of Non-Native Folding Intermediates
Angela M Yu, Paul M. Gasper, Eric J. Strobel, Kyle E. Watters, Alan A. Chen, Julius B. Lucks
bioRxiv 379222; doi: https://doi.org/10.1101/379222

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